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NCT01767285 · ClinicalTrials.gov registry record · Phase 4
Immediate vs. Delayed Postpartum Etonogestrel Implant
A Phase 4 study, sponsored by Duke University.
- Completed
- Registry status
- Phase 4
- Development phase
- 60
- Enrollment target
NCT01767285: Completed Phase 4 study, sponsored by Duke University.
NCT01767285 is a Phase 4 study that has completed, run by Duke University. The registered enrollment target is 60 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (88% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01767285, a Phase 4 study, has completed, sponsored by Duke University.
- COMPLETED
- Registry status
- Phase 4
- Development phase
- 60 participants
- Enrollment target
Study Summary
The investigators are examining if there is a difference in continuation rates of the etonogestrel contraceptive implant between women who have the device placed immediately after delivery, before leaving the hospital, and women who have the device placed at the routine 6-week postpartum visit. There will be 60 subjects total, randomized in a 1:1 ratio, for 30 in each group. All participants will follow-up at the same postpartum clinic 6 weeks after delivery. They will then be contacted at 3, 6, and 12 months postpartum and asked to complete a brief survey. The investigators hypothesize that continuation rates of Implanon will be higher in the immediate postpartum placement arm than in the delayed placement arm.
Primary Outcome
To identify a difference in continuation rates of Implanon® between women who have the device placed immediately postpartum and women who have the device placed at the 6-week postpartum visit.
Interventions
- DRUG Etonogestrel implant
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 60 participants |
| Start Date | 2013-01 |
| Est. Completion | 2015-04 |
| Phase | Phase 4 |
What the finished NCT01767285 record still lists
NCT01767285 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 60 participants, a relatively small participant target, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (88% lower).
The record links to 0 conditions, and to 1 intervention - of which Etonogestrel implant is the first listed.
NCT01767285 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01767285 about?
NCT01767285 is a clinical study titled "Immediate vs. Delayed Postpartum Etonogestrel Implant". The investigators are examining if there is a difference in continuation rates of the etonogestrel contraceptive implant between women who have the device placed immediately after delivery, before leaving the hospital, and women who have the device placed at the routine 6-week postpartum visit. Ther...
What is the current status of trial NCT01767285?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 60 participants. The study started on 2013-01. Estimated completion is 2015-04.
What interventions are being tested in trial NCT01767285?
The interventions under investigation include: Etonogestrel implant (DRUG).
Who is sponsoring clinical trial NCT01767285?
This trial is sponsored by Duke University, which has 1,725 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01767285's enrollment target sits among peer trials
60 1125th of 2000 higher than 799 of 2,000 other Phase 4 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 4 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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